| Weight | 137.964 g/mol |
|---|---|
| Formula | C2H4BrNO |
| Hydrogen Acceptors | 1 |
| Hydrogen Donors | 1 |
| Aromatic Rings | 0 |
| Rotatable Bonds | 1 |
2-Bromoacetamide (683-57-8)
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- Fluorine18 labelling of oligonucleotides: Prosthetic labelling at the 5end using the N(4[18F]fluorobenzyl)2bromoacetamide reagent (Journal of Labelled Compounds and Radiopharmaceuticals, 2003)
- On the Reaction of N-Bromoacetamide with Olefins. Preparation and Chemistry of 2-Bromo-N-Bromoacetimidates, a New Class of Compounds (Canadian Journal of Chemistry, 1971)
- The Addition of N-Bromoacetamide to 2,3-Unsaturated Nitro Sugars, a New Approach to 2,3-Diamino Sugars. Synthesis of Derivatives of 2,3-Diamino-2,3-dideoxy-D-mannose and -D-talose (Canadian Journal of Chemistry, 1974)
- Reactions of Polymers with Reagents Carrying Two Interacting Groups. II. Bromine Displacement from -Bromoacetamide and the Bromoacetate Ion by Poly-(methacrylic Acid) and Poly-(vinylpyridine Betaine)1,2 (Journal of the American Chemical Society, 1959)
- Nucleoside annelating reagents: N-(tert-butoxycarbonyl)-2-bromoacetamide and 2-chloroketene diethyl acetal (Journal of Organic Chemistry, 1985)
- Automated radiosynthesis of N(4[18F]fluorobenzyl)2bromoacetamide: an F18labeled reagent for the prosthetic radiolabeling of oligonucleotides (Journal of Labelled Compounds and Radiopharmaceuticals, 2008)
-
Predict GHS Hazards for Any Chemical in silico.
Including Acute Oral Tox, Skin Sensitization, Eye Irritation, Aquatic Tox, & more. -
SMILESC(C(=O)N)Br
-
InChIKeyJUIKUQOUMZUFQT-UHFFFAOYSA-N
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Synthesis
Reactant
+
dimethyl sulfide
(Corey-Kim oxidation of secondary alcohols)
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2-Bromoacetamide
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